"Twisted" conjugated molecules as donor materials for efficient all-small-molecule organic solar cells processed with tetrahydrofuran

被引:37
|
作者
Cheng, Xiafei [1 ]
Li, Miaomiao [1 ,2 ]
Guo, Ziqi [4 ]
Yu, Jinde [5 ,6 ]
Lu, Guanghao [5 ,6 ]
Bu, Laju [5 ,6 ]
Ye, Long [7 ]
Ade, Harald [7 ]
Chen, Yongsheng [4 ]
Geng, Yanhou [1 ,2 ,3 ]
机构
[1] Tianjin Univ, Sch Mat Sci & Engn, Tianjin 300072, Peoples R China
[2] Tianjin Univ, Collaborat Innovat Ctr Chem Sci & Engn, Tianjin Key Lab Mol Optoelect Sci, Tianjin, Peoples R China
[3] Int Campus Tianjin Univ, Joint Sch Natl Univ Singapore & Tianjin Univ, Fuzhou 350207, Fujian, Peoples R China
[4] Nankai Univ, State Key Lab & Inst Elementoorgan Chem, Ctr Nanoscale Sci & Technol, Key Lab Funct Polymer Mat,Coll Chem, Tianjin 300071, Peoples R China
[5] Xi An Jiao Tong Univ, Frontier Inst Sci & Technol, Xian 710049, Shaanxi, Peoples R China
[6] Xi An Jiao Tong Univ, Sch Sci, Xian 710049, Shaanxi, Peoples R China
[7] North Carolina State Univ, Organ & Carbon Elect Lab ORaCEL, Dept Phys, Raleigh, NC 27695 USA
基金
中国国家自然科学基金;
关键词
POWER CONVERSION EFFICIENCY; RING ELECTRON-ACCEPTOR; DESIGN STRATEGY; POLYMER; FULLERENE; SOLVENT; PERFORMANCE; GENERATION;
D O I
10.1039/c9ta07760j
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
High-performance organic semiconductors that can be processed with environmentally benign solvents are highly desirable for printable optoelectronics. Herein, four acceptor-donor-acceptor conjugated molecules, i.e., DRTT-T, DRTT-R, DRTT-OR and DRTT, with 3-ethylrhodanine as acceptor terminal units and 2,5-bis(4,8-di(5-(2-ethylhexyl)thiophen-2-yl)benzo[1,2-b:4,5-b ']dithiophen-2-yl)thieno[3,2-b]thiophene derivatives as donor units were synthesized. 5-(2-Ethylhexyl)thiophen-2-yl, 2-ethylhexyl and 2-ethylhexyloxy were introduced at the beta-positions of the central thieno[3,2-b]thiophene (TT) units in DRTT-T, DRTT-R and DRTT-OR, respectively, and unsubstituted TT was used as the central unit in DRTT. As revealed by density functional theory calculations, DRTT-OR and DRTT adopt an almost planar geometry, while DRTT-T and DRTT-R have "twisted" backbones due to the introduction of bulky substituents on TT units. Differing from DRTT-OR and DRTT which are only well soluble in chlorinated solvents such as chloroform, DRTT-T and DRTT-R also show high solubility in "greener" solvents, including toluene and tetrahydrofuran (THF). Non-fullerene small molecule (NFSM) organic solar cells (OSCs) were fabricated with these molecules as donor materials. The molecules (DRTT-T and DRTT-R) with twisted backbones displayed remarkably higher device performance compared to more planar ones (DRTT-OR and DRTT), attributed to the formation of ordered face-on microstructures with pi-pi stacking distances of 3.7-3.8 angstrom and interpenetration networks of donor and acceptor components in the blend films based on DRTT-T and DRTT-R. Most importantly, the power conversion efficiencies (PCEs) of DRTT-T and DRTT-R based devices processed with THF reached 9.37% and 10.45%, respectively. This study demonstrates that "twisting" conjugated backbones is an appropriate strategy to design eco-friendly solvent processable organic semiconductors for high-efficiency OSCs.
引用
收藏
页码:23008 / 23018
页数:11
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